Announcing two new gene level annotators from the Network of Cancer Genes & Healthy Drivers. The Network of Cancer Genes…
Latest Release
Variant interpretation is central to genomic medicine, but one of its most debated areas is how to use computational evidence….
As a part of our ongoing effort to update our variant effect predictors with calibration for ACMG/AMP classifications, we have…
On the final day of OpenCRAVAT’s Adventurer’s Guide, we celebrate you—our community. OpenCRAVAT thrives because of the passion, creativity, and…
OpenCRAVAT is designed with flexibility in mind, offering users the ability to tailor their genomic variant analyses to specific research…
On the sixth day of OpenCRAVAT, we’re highlighting six essential tools that transform your genomic data into actionable insights. These…